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MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
VOMITING ( 3 FDA reports)
TREMOR ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
FALL ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
TIC ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
METASTASES TO FALLOPIAN TUBE ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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